Canonical Allele Identifier: CA2317520187

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105845_1105849delinsTGGGG , CM000681.2:g.1105845_1105849delinsTGGGG	GRCh38
NC_000019.9:g.1105844_1105848delinsTGGGG , CM000681.1:g.1105844_1105848delinsTGGGG	GRCh37
NC_000019.8:g.1056844_1056848delinsTGGGG	NCBI36
NG_050621.1:g.6920_6924delinsTGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.587+36_587+40delinsTGGGG	ENSP00000473614.3:n.587+36_587+40delinsTGGGG
ENST00000593032.6:c.395+36_395+40delinsTGGGG	ENSP00000465828.4:n.395+36_395+40delinsTGGGG
ENST00000706713.1:c.470+36_470+40delinsTGGGG	ENSP00000516510.1:n.470+36_470+40delinsTGGGG
ENST00000706714.1:c.395+36_395+40delinsTGGGG	ENSP00000516511.1:n.395+36_395+40delinsTGGGG
ENST00000706715.1:c.92+36_92+40delinsTGGGG	ENSP00000516512.1:n.92+36_92+40delinsTGGGG
ENST00000354171.13:c.476+36_476+40delinsTGGGG MANE Select	ENSP00000346103.7:n.476+36_476+40delinsTGGGG
ENST00000589115.6:c.476+36_476+40delinsTGGGG	ENSP00000466872.3:n.476+36_476+40delinsTGGGG
ENST00000354171.12:c.476+36_476+40delinsTGGGG	ENSP00000346103.7:n.476+36_476+40delinsTGGGG
ENST00000585480.1:c.209+36_209+40delinsTGGGG	ENSP00000467900.1:n.209+36_209+40delinsTGGGG
ENST00000587648.5:c.356+36_356+40delinsTGGGG	ENSP00000468349.1:n.356+36_356+40delinsTGGGG
ENST00000588919.5:c.395+36_395+40delinsTGGGG	ENSP00000464989.3:n.395+36_395+40delinsTGGGG
ENST00000589115.5:c.476+36_476+40delinsTGGGG	ENSP00000466872.2:n.476+36_476+40delinsTGGGG
ENST00000592940.2:n.451_455delinsTGGGG
ENST00000593032.5:c.395+36_395+40delinsTGGGG	ENSP00000465828.3:n.395+36_395+40delinsTGGGG
ENST00000611653.4:c.395+36_395+40delinsTGGGG	ENSP00000483655.1:n.395+36_395+40delinsTGGGG
ENST00000616066.4:c.473+36_473+40delinsTGGGG	ENSP00000485000.1:n.473+36_473+40delinsTGGGG
ENST00000622390.4:c.584+36_584+40delinsTGGGG	ENSP00000477503.1:n.584+36_584+40delinsTGGGG
NM_001039847.2:c.476+36_476+40delinsTGGGG	NP_001034936.1:n.476+36_476+40delinsTGGGG
NM_001039848.2:c.587+36_587+40delinsTGGGG	NP_001034937.1:n.587+36_587+40delinsTGGGG
NM_002085.4:c.476+36_476+40delinsTGGGG	NP_002076.2:n.476+36_476+40delinsTGGGG
NM_001039848.3:c.587+36_587+40delinsTGGGG	NP_001034937.1:n.587+36_587+40delinsTGGGG
NM_001039847.3:c.476+36_476+40delinsTGGGG	NP_001034936.1:n.476+36_476+40delinsTGGGG
NM_001039848.4:c.587+36_587+40delinsTGGGG	NP_001034937.1:n.587+36_587+40delinsTGGGG
NM_001367832.1:c.395+36_395+40delinsTGGGG	NP_001354761.1:n.395+36_395+40delinsTGGGG
NM_002085.5:c.476+36_476+40delinsTGGGG MANE Select	NP_002076.2:n.476+36_476+40delinsTGGGG